Vale M G
Biochem Pharmacol. 1985 Dec 15;34(24):4245-9. doi: 10.1016/0006-2952(85)90279-5.
The effect of phenothiazines (trifluoperazine and chlorpromazine) on the activity of the sarcoplasmic reticulum Ca2+ pump was investigated. These drugs have a biphasic action on the ATPase activity. They inhibit the enzyme at high concentrations, but below 150 microM, they promote a significant stimulation of the ATP hydrolysis, which is accompanied by a slight increase of the Ca2+ transport. Leaking of the membrane occurs only at drug concentrations above 150 microM. The phenothiazine stimulatory effect was not found in the isolated enzyme whose activity was inhibited at all concentrations studied. These results indicate that low concentrations of phenothiazines uncouple the sarcoplasmic reticulum Ca2+ pump without disrupting the membrane and that the drug stimulatory effect on the ATPase is not due to a direct interaction with the enzyme. It is suggested that a coupling factor or a specific microenvironment surrounding the enzyme regulates the association between the Ca2+ transport and the ATP hydrolysis by sarcoplasmic reticulum of the skeletal muscle cell.
研究了吩噻嗪类药物(三氟拉嗪和氯丙嗪)对肌浆网Ca2+泵活性的影响。这些药物对ATP酶活性具有双相作用。它们在高浓度时抑制该酶,但在低于150微摩尔时,它们会显著促进ATP水解,同时伴随着Ca2+转运略有增加。仅在药物浓度高于150微摩尔时膜才会发生渗漏。在所研究的所有浓度下活性均受到抑制的分离酶中未发现吩噻嗪的刺激作用。这些结果表明,低浓度的吩噻嗪可使肌浆网Ca2+泵解偶联而不破坏膜,且药物对ATP酶的刺激作用并非由于与该酶的直接相互作用。有人提出,一种偶联因子或酶周围的特定微环境调节骨骼肌细胞肌浆网的Ca2+转运与ATP水解之间的关联。